6-Methylpyridine-2-carboxaldehyde丨CAS 1122-72-1

6-Methylpyridine-2-carboxaldehyde丨CAS 1122-72-1
Product Introduction:
Catalog No.: SS088163
CAS No.: 1122-72-1
Purity(GC): 98% min
Product Name: 6-Methylpyridine-2-carboxaldehyde
Molecular Formula: C7H7NO
Molecular Weight: 121.14
Synonym(s): 6-Methyl-2-pyridinecarboxaldehyde; 2-Picoline-6-carboxaldehyde
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Technical Parameters
Description

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Specifications

 

Appearance: Light yellow to yellow crystals
Purity (GC): 98% min
Single impurity: 0.5% max
M.P: 33-35℃
Water (KF): 0.5% max

 

 

 

Applications

1. Pharmaceutical Intermediate

Used in the synthesis of pharmaceutical compounds, especially heterocyclic drugs.

The aldehyde group is reactive and enables formation of Schiff bases, imines, and other nitrogen-containing heterocycles.

2. Organic Synthesis

Serves as a versatile building block in fine chemical synthesis.

Used to prepare ligands, coordination compounds, and other functionalized pyridine derivatives.

3. Coordination Chemistry

The compound can act as a bidentate ligand through the aldehyde oxygen and the pyridine nitrogen, useful in metal complex formation.

4. Material Science

Utilized in the design and synthesis of functional materials, including sensors and catalysts.

Benefits

High Reactivity: The aldehyde functional group allows for diverse chemical modifications.

Structural Versatility: Combines the chemical properties of pyridine and aldehyde, useful for multi-functional molecules.

Facilitates Ligand Design: Enables synthesis of chelating ligands important in catalysis and coordination chemistry.

Widely Used in Research: A valuable intermediate for medicinal chemistry and materials science.

Conclusion

6-Methylpyridine-2-carboxaldehyde (CAS 1122-72-1) is an important heterocyclic aldehyde extensively used as an intermediate in pharmaceuticals, organic synthesis, and coordination chemistry. Its dual functional groups provide versatility for chemical modifications and complex molecule design. This compound continues to be essential for developing new drugs and functional materials.

 

 

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